Canonical Allele Identifier: CA2766242753
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857774G>C , CM000686.2:g.12857774G>C GRCh38
NC_000024.9:g.14969699G>C , CM000686.1:g.14969699G>C GRCh37
NC_000024.8:g.13479093G>C NCBI36
NG_008311.1:g.161540G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7530+113G>C ENSP00000498372.1:n.7530+113G>C
ENST00000338981.7:c.7530+113G>C MANE Select ENSP00000342812.3:n.7530+113G>C
ENST00000426564.6:n.7557+113G>C
ENST00000453031.1:c.575+113G>C
ENST00000471409.1:n.849+113G>C
NM_004654.3:c.7530+113G>C NP_004645.2:n.7530+113G>C
XM_011531469.1:c.7530+113G>C XP_011529771.1:n.7530+113G>C
XM_011531470.1:c.7296+113G>C XP_011529772.1:n.7296+113G>C
XM_017030078.2:c.7545+113G>C XP_016885567.1:n.7545+113G>C
NM_004654.4:c.7530+113G>C MANE Select NP_004645.2:n.7530+113G>C